by Dr. C.H. Weaver M.D. updated 5/2019
Imlygic® (talimogene laherparepvec), the first ever FDA-approved oncolytic virus therapy, has been approved for the treatment of melanoma.
The approval is for the treatment of melanoma sites in the skin and lymph nodes that cannot be surgically removed. Imlygic is given as an injection directly into the site of cancer, and is given through a series of injections over the course of 6 months.
Melanoma is a type of skin cancer that typically starts in the form of a mole. If caught and treated early with surgical removal, cure rates remain high. However, if melanoma spreads outside its site of origin, especially if it has spread to other sites in the body, it can become deadly.
Melanoma has been difficult to treat in the past, as it did not respond well to standard chemotherapy and/or radiation therapy. However, researchers have recently developed newer agents which create improved anti-cancer responses and overall outcomes for patients with this disease.
Imlygic is a genetically modified live oncolytic herpes virus therapy. In essence, Imlygic consists of a herpes virus that has been genetically modified through laboratory processes. Imlygic is injected into the site of the cancer where the modified herpes virus replicates inside cancer cells and causes the cancer cells to rupture and die.
The clinical trial leading to the approval of Imlygic included 436 patients with melanoma that had spread to distant sites in the body and could not be surgically removed. Patients were treated with Imlygic or a comparator therapy for at least 6 months, unless there were no visible melanoma sites left and directly compared. The patients had Stage IIIB, IIIC, or IV melanoma that could not be surgically removed. Patients were treated with either T-VEC or GM-CSF for up to 18 months.
The primary outcome of interest was a durable response (a partial or complete elimination of cancer that lasted for at least six months).
- Durable responses occurred in 16% of patients in the T-VEC group and 2% of patients in the GM-CSF group. In the T-VEC group, durable responses were most common among patients with Stage III melanoma.
- The overall response rate was 26% among patients in the T-VEC group and 6% among patients in the GM-CSF group.
- The most common side effects of T-VEC were fatigue, chills, and fever.
- Using data from the phase III study presented at ASCO in 2013, researchers analyzed 3,219 tumor lesions (in 286 patients) to study the response to the drug in injected versus non-injected tumors. Overall, 2,043 lesions were injected with T-VEC at least once, 1,022 were un-injected non-visceral, and 154 were un-injected visceral lesions.
- The results showed that 64 percent of injected tumors shrank by half, while 32 percent of un-injected non-visceral and 16 percent of un-injected visceral lesions shrank by half.
- A total of 6 patients converted from inoperable to operable melanoma after receiving T-VEC. In total, 37 surgeries were performed during the course of the trial: 15 resulted in no evidence of disease and 3 showed a pathologic complete response.
- The vaccine shrank tumors that were directly injected as well as those that were not injected—indicating that the vaccine was triggering the immune system to fight the distant tumors. The researchers concluded that this promising new agent warrants further study.
Overall 16.3% of patients treated with Imlygic experienced a decrease in the size of their melanoma sites in the skin and lymph nodes for at least 6 months, compared to only 2,1% of patients treated with the comparator therapy. The therapy was generally well tolerated and the most common side effects were flu-like symptoms and pain at the injection site.
Results show sustained effectiveness of disease response and favorable side effect profile.
From the Amer College of Surgeons 1/2019
Injection of a genetically modified virus that induces the body’s own immune cells to attack metastatic melanoma effectively treated almost 40 percent of patients with tumors that could not be surgically removed, according to researchers from three prominent cancer centers in a study published on the Journal of the American College of Surgeons website in advance of print publication.
“Our findings in the real world mimic what the clinical trials have found,” said corresponding author David W. Ollila, MD, FACS, a general surgical oncologist, department of surgery, University of North Carolina at Chapel Hill. “It’s a different world now in metastatic melanoma, because instead of the traditional cytotoxic chemotherapy that not only kills cancer cells but also kills normal cells, we’re stimulating the immune system to attack the cancer cells.”
The researchers evaluated 80 adult patients treated with talimogene laherparepvec (TVEC, sold under the brand name Imlygic, by AMGEN Inc.) over a three-year period ending October 1, 2018. The Food and Drug Administration approved TVEC in 2015 for the treatment of stage IIIB to advanced-stage IV metastatic melanoma. TVEC is a genetically modified herpes virus that contains the stimulatory factor known as GM-CSF that increases a tumor-specific immune response.
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TVEC is injected directly into the skin tumor in the physician’s office or clinic and the patient may leave immediately afterward, without the severe side effects of chemotherapy or other cancer drugs that act on the body’s immune system. The stimulatory factor sends a signal to attract white blood cells into the tumor, Dr. Ollila explained, thereby inducing the body’s activated immune system to kill the metastatic melanoma cells.
The researchers reported that 46 percent of participants (37 patients) had stage IIIB disease, 31 percent (25) had stage IIIC disease, 1 percent (1) had clinical stage IIID disease, and 20 percent (16) had cancer that spread to a distant site at the time of treatment. Patients received a median of five cycles of TVEC. Most study patients—57 percent—received some form of therapy before enrollment in the study.
The researchers found that 39 percent of participants (31 patients) had a complete local response to TVEC therapy, and 18 percent (14 patients) had a partial response. “It’s pretty hard to ignore a response rate of 39 percent,” Dr. Ollila said. He noted that patients with stage IIIB disease had an even higher complete local response rate of 68 percent, compared with those with higher-stage disease: 26 percent for IIIC, 0 percent for IIID, and 6 percent for IV. At a median follow-up of 12 months, 59 percent of patients with stage IIIB disease showed no signs of recurrent disease.
Dr. Ollila noted that these findings surpass those from the clinical trial that led to the approval of TVEC. The overall response rate from the clinical trial was 26.4 percent.* However, that trial included a higher percentage of patients with cancer that had spread to other organs, including the lungs.
TVEC was also well tolerated by the study patients, Dr. Ollila said. Side effects were mild and self-limited; the most common side effects were flu-like symptoms in 28 percent of participants (22 patients), whereas the side effects of chemotherapy and other drugs that activate the body’s immune system can be severe, including nausea or vomiting and immune-related toxicities. Only five patients stopped treatment for a variety of complications, including cold sores or infection.
One key takeaway from the study was that patients with stage IIIB/C or stage M1A metastatic melanoma may benefit more from the drug than those with higher stage cancers, Dr. Ollila said. “We reported a complete response rate that was higher than the 2015 clinical trial because the clinical trial included higher-risk patients in whom TVEC may have limited effectiveness,” he said.
These study results raise the question of administering TVEC with other anti-cancer treatments, including drugs that inhibit the growth of other types of skin cancer cells. “Can we now use TVEC in combination with these drugs and drive the response rates even higher?” Dr. Ollila said. “Could the same principle work in metastatic merkel cell and locally advanced squamous cell carcinoma?” The latter is the focus of an ongoing clinical trial in which Dr. Ollila and his co-authors are participating.
Besides chemotherapy, another existing treatment for skin cancer is surgical removal of the tumor, but that too can be problematic, Dr. Ollila said. “We know that surgeons will eventually reach a point where surgical resection is no longer feasible.” The most compelling finding of the study is that it supports TVEC injection as an option for melanoma. “It appears that there’s no role for traditional chemotherapy any longer for treating this disease,” Dr. Ollila added.
Jonathan S. Zager, MD, FACS, of Moffitt Cancer Center, Tampa, Fla., and Keith A. Delman, MD, FACS, of Emory University School of Medicine, Atlanta, Ga., directed the study at their centers and are lead coauthors with Dr. Ollila.
Along with Drs. Zager and Delman, Dr. Ollila’s coauthors are Raphael J. Louie, MD, of the department of surgery, and Frances Collichio, MD, of the department of medicine, at UNC; Matthew C. Perez, MD, Amod A. Sarnaik, MD, FACS, and James Sun, MD, of Moffitt Cancer Center; and Mohammad Raheel Jajja, MD,,and Michael Lowe, MD, FACS, of Emory University.
Dr. Zager disclosed relationships with Amgen, Array BioPharma, Merck, Delcath Systems, Philogen, Castle Biosciences and Provectus Biopharmaceuticals; Dr. Collichio disclosed relationships with Amgen and Novartis; Dr. Perez disclosed a relationship with Amgen; and Dr. Sarniak disclosed relationships with Iovance Biotherapeutics, B4CC Inc., and Provectus. Dr. Ollila and the other study co-authors have no relevant relationships to disclose.
Reference: Real World Outcomes of Talimogene Laherparepvec Therapy: A Multi-Institutional Experience. Journal of the American College of Surgeons. Available [here](https://www.journalacs.org/article/S1072-7515(19%2930024-9/fulltext)
Reference: United States Food and Drug Administration. News Release. FDA approves first-of-its-kind product for the treatment of melanoma. Available at: fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm469571.htm. Accessed October 27, 2015.